Microscale magnetic microparticle-based immunopurification of cytokinins from Arabidopsis root apex

被引:15
作者
Plackova, Lenka [1 ,2 ]
Oklestkova, Jana [1 ]
Pospiskova, Kristyna [3 ]
Polakova, Katerina [3 ]
Bucek, Jan [2 ]
Styskala, Jakub [4 ]
Zatloukal, Marek [2 ]
Safarik, Ivo [3 ,5 ]
Zboril, Radek [3 ]
Strnad, Miroslav [1 ]
Dolezal, Karel [1 ,2 ]
Novak, Ondrej [1 ]
机构
[1] Palack Univ& Inst Expt Bot, Czech Acad Sci,Fac Sci, Ctr Reg Hana Biotechnol & Agr Res, Lab Growth Regulators, Olomouc 78371, Czech Republic
[2] Palacky Univ, Fac Sci, Ctr Reg Hana Biotechnol & Agr Res, Dept Chem Biol & Genet, Olomouc 78371, Czech Republic
[3] Palack Univ, Reg Ctr Adv Technol & Mat, Slechtitelu 27, Olomouc 78371, Czech Republic
[4] Palack Univ, Fac Sci, Dept Organ Chem, 17 Listopadu 12, Olomouc 77146, Czech Republic
[5] CAS, ISB, Biol Ctr, Dept Nanobiotechnol, Na Sadkach 7,, Ceske Budejovice 37005, Czech Republic
关键词
cytokinins; magnetic microparticles; immunoaffinity separation; metabolite profiling; Arabidopsis thaliana; technical advance; SOLID-PHASE EXTRACTION; TANDEM MASS-SPECTROMETRY; ENDOGENOUS CYTOKININS; PLANT-SAMPLES; CIS-ZEATIN; QUANTITATIVE-ANALYSIS; AROMATIC CYTOKININS; ABSCISIC-ACID; ORYZA-SATIVA; PURIFICATION;
D O I
10.1111/tpj.13443
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Cytokinins (CKs) are pivotal plant hormones that have crucial roles in plant growth and development. However, their isolation and quantification are usually challenging because of their extremely low levels in plant tissues (pmol g(-1) fresh weight). We have developed a simple microscale magnetic immunoaffinity-based method for selective one-step isolation of CKs from very small amounts of plant tissue (less than 0.1 mg fresh weight). The capacity of the immunosorbent and the effect of the complex plant matrix on the yield of the rapid one-step purification were tested using a wide range of CK concentrations. The total recovery range of the new microscale isolation procedure was found to be 30-80% depending on individual CKs. Immunoaffinity extraction using group-specific monoclonal CK antibodies immobilized onto magnetic microparticles was combined with a highly sensitive ultrafast mass spectrometry-based method with a detection limit close to one attomole. This combined approach allowed metabolic profiling of a wide range of naturally occurring CKs (bases, ribosides and N-9-glucosides) in 1.0-mm sections of the Arabidopsis thaliana root meristematic zone. The magnetic immunoaffinity separation method was shown to be a simple and extremely fast procedure requiring minimal amounts of plant tissue.
引用
收藏
页码:1065 / 1075
页数:11
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